ENST00000380036.10:c.2730T>C
MANE Select
|
ENSP00000369375.4:p.Leu910=
|
|
ENST00000380036.8:c.2730T>C
|
ENSP00000369375.4:p.Leu910=
|
|
ENST00000406359.8:c.2601T>C
|
ENSP00000383977.4:p.Leu867=
|
|
ENST00000519097.5:c.2286T>C
|
ENSP00000430686.1:p.Leu762=
|
|
ENST00000615002.4:c.*1231T>C
|
ENSP00000480251.1:n.*1231T>C
|
|
NM_000459.4:c.2730T>C
|
NP_000450.2:p.Leu910=
|
|
NM_001290077.1:c.2601T>C
|
NP_001277006.1:p.Leu867=
|
|
NM_001290078.1:c.2286T>C
|
NP_001277007.1:p.Leu762=
|
|
XM_005251561.1:c.2727T>C
|
XP_005251618.1:p.Leu909=
|
|
XM_005251563.1:c.2598T>C
|
XP_005251620.1:p.Leu866=
|
|
XM_005251561.2:c.2727T>C
|
XP_005251618.1:p.Leu909=
|
|
XM_005251563.2:c.2598T>C
|
XP_005251620.1:p.Leu866=
|
|
NM_000459.5:c.2730T>C
MANE Select
|
NP_000450.3:p.Leu910=
|
|
NM_001375475.1:c.2727T>C
|
NP_001362404.1:p.Leu909=
|
|
NM_001375476.1:c.2598T>C
|
NP_001362405.1:p.Leu866=
|
|